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汉黄芩素通过双重靶向抑制肺炎链球菌溶血素和转肽酶 A 来减弱肺炎链球菌的致病性。

Wogonin attenuates the pathogenicity of Streptococcus pneumoniae by double-target inhibition of Pneumolysin and Sortase A.

机构信息

Changchun University of Chinese Medicine, Changchun, China.

Affiliated Hospital to Changchun University of Chinese Medicine, Jilin, China.

出版信息

J Cell Mol Med. 2023 Feb;27(4):563-575. doi: 10.1111/jcmm.17684. Epub 2023 Feb 6.

Abstract

Streptococcus pneumoniae (S. pneumoniae) is a major causative agent of respiratory disease in patients and can cause respiratory distress and other symptoms in severe cases. Pneumolysin (PLY) is a pore-forming toxin that induces host tissue injury and inflammatory responses. Sortase A (SrtA), a catalytic enzyme that anchors surface-associated virulence factors, is critical for S. pneumoniae virulence. Here, we found that the active ingredient of the Chinese herb Scutellaria baicalensis, wogonin, simultaneously inhibited the haemolytic activity of PLY and SrtA activity. Consequently, wogonin decreased PLY-mediated cell damage and reduced SrtA-mediated biofilm formation by S. pneumoniae. Furthermore, our data indicated that wogonin did not affect PLY expression but directly altered its oligomerization, leading to reduced activity. Furthermore, the analysis of a mouse pneumonia model further revealed that wogonin reduced mortality in mice infected with S. pneumoniae laboratory strain D39 and S. pneumoniae clinical isolate E1, reduced the number of colony-forming units in infected mice and decreased the W/D ratio and levels of the inflammatory factors TNF-α, IL-6 and IL-1β in the lungs of infected mice. Thus, wogonin reduces S. pneumoniae pathogenicity by inhibiting the dual targets PLY and SrtA, providing a treatment option for S. pneumoniae infection.

摘要

肺炎链球菌(S. pneumoniae)是导致患者呼吸道疾病的主要病原体,严重情况下可引起呼吸窘迫等症状。肺炎球菌溶血素(PLY)是一种形成孔的毒素,可诱导宿主组织损伤和炎症反应。表面相关毒力因子的锚定催化酶天冬酰胺酰内肽酶 A(SrtA)对肺炎链球菌的毒力至关重要。在这里,我们发现中国草药黄芩的有效成分黄芩素同时抑制了 PLY 的溶血活性和 SrtA 活性。因此,黄芩素降低了 PLY 介导的细胞损伤,并减少了 S. pneumoniae 介导的生物膜形成。此外,我们的数据表明,黄芩素不影响 PLY 的表达,而是直接改变其寡聚化,从而降低其活性。此外,肺炎小鼠模型的分析进一步表明,黄芩素降低了感染实验室株 D39 和临床分离株 E1 的肺炎链球菌小鼠的死亡率,减少了感染小鼠肺部的菌落形成单位数量,并降低了 TNF-α、IL-6 和 IL-1β 等炎症因子的 W/D 比值和水平。因此,黄芩素通过抑制 PLY 和 SrtA 这两个双重靶点降低了肺炎链球菌的致病性,为肺炎链球菌感染提供了一种治疗选择。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0116/9930429/a7248742cc54/JCMM-27-563-g004.jpg

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